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hereditary sensory and autonomic neuropathy type 1A (DOID:0070152)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type IA; HSAN1A
Alt IDs: OMIM:162400
Definition: A hereditary sensory and autonomic neuropathy type 1 characterized by onset of sensorimotor axonal neuropathy in the first or second decades of life that has_material_basis_in heterozygous mutation in the SPTLC1 gene on chromosome 9q22.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/24/2023
MGI 6.22
The Jackson Laboratory